Canonical Allele Identifier: CA2574622141
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762631-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762631C>A , CM000672.2:g.94762631C>A GRCh38
NC_000010.10:g.96522388C>A , CM000672.1:g.96522388C>A GRCh37
NC_000010.9:g.96512378C>A NCBI36
NG_008384.2:g.4926C>A
NG_008384.3:g.4951C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-75C>A ENSP00000360372.3:n.-75C>A
ENST00000464755.1:c.932-12427C>A ENSP00000483243.1:n.932-12427C>A
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